Deuterated etifoxine is under clinical development by GABA Therapeutics and currently in Phase I for Social Anxiety Disorder (SAD/Social Phobia). According to GlobalData, Phase I drugs for Social Anxiety Disorder (SAD/Social Phobia) does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Deuterated etifoxine LoA Report. Buy the report here.

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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Deuterated etifoxine overview

Deuterated etifoxine is under development for the treatment of neuropathic and inflammatory pain, multiple sclerosis, epilepsy, generalized anxiety disorder, social anxiety disorder (SAD), post partum depression (PPD), panic disorder, essential tremor, depression, Alzheimer’s disease, stroke, traumatic brain injury, nerve/spinal cord injury and retinal/macular degeneration. Deuterated etifoxine is a version of racemic etifoxine. It is administered through oral route. It is developed based on allosteric modulation technology. It acts by targeting GABAA receptors and TSPO. D-etifoxine is a new chemical entity (NCE).
It was also under development for the treatment of autism spectrum disorders(ASD), pediatric epilepsy, post-traumatic stress disorder (PTSD), major depressive disorder (MDD) and treatment resistant depression (TRD)

GABA Therapeutics overview

Gaba Therapeutics is a therapeutic company that develops anxiety medications. The company is headquartered in Newport Beach, California, the US

For a complete picture of Deuterated etifoxine’s drug-specific PTSR and LoA scores, buy the report here.

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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.